Pharmaceutical Technology and Drug Delivery, Department of Pharmacy, Universitas Sebelas Maret, Surakarta, Indonesia.
Department of Pharmaceutics, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Drug Dev Ind Pharm. 2020 Jan;46(1):146-158. doi: 10.1080/03639045.2019.1711387.
The aim of this research was to assess the effect of polymer blend and effervescent components on the floating and swelling behaviors of swellable gastro-floating formulation as well as the drug release through a compartmental modeling analysis. Swellable gastro-floating formulation of freely water-soluble drug, metformin HCl as a drug model, was formulated and developed using D-optimal design. Polymer combination between interpolymer complex (IPC) (poly-vinyl acetate-copolymer methacrylate) and hydroxy propyl methyl cellulose (HPMC), and effervescent components were studied and optimized in this work. Several factors affecting the drug release behavior were determined e.g. swelling behavior, erosion behavior, and floating behavior were studied as well as the drug release through compartmental modeling analysis. The results revealed that the hydrophilic polymer was responsible for gas entrapment formed from effervescent reaction, meanwhile IPC contributed on maintaining the swollen matrix integrity through intermolecular polymer interaction. In addition, effervescent components played fundamental role in the formation of porous system as well as inducing burst release effect. Compartmental modeling provided different outlook about the drug release. Presence of IPC at a high proportion (10-15%) of the polymer blend modulated the changes of pattern of the drug release kinetics and mechanism. Finally, compartmental modeling-based approach was more adequate to describe the drug release kinetics and mechanism compared to the monophasic equation model correlating with process understanding of the drug release from swellable gastro-floating formulation.
本研究旨在评估聚合物共混物和泡腾成分对可膨胀胃漂浮制剂的漂浮和膨胀行为以及通过区室模型分析的药物释放的影响。以盐酸二甲双胍(freely water-soluble drug)为药物模型,采用 D-最优设计,制备并开发了可膨胀胃漂浮制剂。本研究研究并优化了聚合物共混物(interpolymer complex(IPC)(聚醋酸乙烯酯-共聚物甲基丙烯酸酯)和羟丙基甲基纤维素(HPMC)之间的聚合物组合以及泡腾成分。确定了影响药物释放行为的几个因素,例如膨胀行为、侵蚀行为和漂浮行为,以及通过区室模型分析的药物释放。结果表明,亲水性聚合物负责泡腾反应形成的气体夹带,而 IPC 通过分子间聚合物相互作用有助于维持膨胀基质的完整性。此外,泡腾成分在形成多孔系统和诱导突释效应方面发挥了重要作用。区室模型提供了药物释放的不同视角。IPC 以聚合物共混物的高比例(10-15%)存在时,调节了药物释放动力学和机制的变化模式。最后,与可膨胀胃漂浮制剂中药物释放的过程理解相关的单相方程模型相比,基于区室模型的方法更适合描述药物释放动力学和机制。